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Details
Link-It Detail - Human Phenotype - Abnormality of cells of the lymphoid lineage
Debug Stats
  • ### Total Build Time: 28 ms 19.702 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 219 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 257 bytes
  • Skipping details on: CONCEPT_SYNONYM gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_SEMANTIC_TYPE gt=0 Completed: 0 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=5 ms Completed: 5 ms rowSize= 463 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 750 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=3 ms Completed: 3 ms rowSize= 1.178 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=13 ms Completed: 13 ms rowSize= 15.692 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.038 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of cells of the lymphoid lineage HP:0012140
Definition (1)
An anomaly of cells that originate from the `lymphoid lineage restricted progenitor cell` (CL:0000838).
Parents (1)
img Abnormality of bone marrow cell morphology HP:0005561
Children (2)
img Lymphocvtosis HP:0012141
img Lymphopenia HP:0001888
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001185img Abnormality of bone marrow cell morphology HP:0005561
Genes (68)

Species:
human : 68
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanMPDMRS574047Martin-Probst deafness-mental retardation syndrome
HumanMMAB326625methylmalonic aciduria (cobalamin deficiency) cblB type
HumanRAB40AL282808RAB40A, member RAS oncogene family-like
HumanMMAA166785methylmalonic aciduria (cobalamin deficiency) cblA type
HumanCCBE1147372collagen and calcium binding EGF domains 1
img HP RolledUp, OMIM ID: 235510
HumanG6PC392579glucose 6 phosphatase, catalytic, 3
img HP RolledUp, OMIM ID: 612541
HumanNHEJ179840nonhomologous end-joining factor 1
img HP RolledUp, OMIM ID: 611291
HumanPALB279728partner and localizer of BRCA2
img HP RolledUp, OMIM ID: 610832
HumanNOD264127nucleotide-binding oligomerization domain containing 2
HumanPDSS257107prenyl (decaprenyl) diphosphate synthase, subunit 2
HumanCOQ957017coenzyme Q9 homolog (S. cerevisiae)
HumanADCK356997aarF domain containing kinase 3
HumanBTNL256244butyrophilin-like 2 (MHC class II associated)
HumanLMBRD155788LMBR1 domain containing 1
HumanNHP255651NHP2 ribonucleoprotein
HumanCHD755636chromodomain helicase DNA binding protein 7
img HP RolledUp, OMIM ID: 214800
HumanNOP1055505NOP10 ribonucleoprotein
HumanWRAP5355135WD repeat containing, antisense to TP53
HumanAPTX54840aprataxin
HumanSBDS51119Shwachman-Bodian-Diamond syndrome
HumanSMARCAL150485SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a-like 1
img HP RolledUp, OMIM ID: 242900
HumanOSTM128962osteopetrosis associated transmembrane protein 1
HumanCOQ227235coenzyme Q2 4-hydroxybenzoate polyprenyltransferase
HumanTINF226277TERF1 (TRF1)-interacting nuclear factor 2
img HP RolledUp, OMIM ID: 127550
HumanPDSS123590prenyl (decaprenyl) diphosphate synthase, subunit 1
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0012140Abnormality of cells of the lymphoid lineage0self